01 4AAIPHARMA LLC
02 4ALKEM LABS LTD
03 3AMNEAL
04 1CASPER PHARMA LLC
05 1HIKMA
06 2LEGACY PHARMA
07 1QUAD PHARMS
08 1RISING
09 4ZYDUS PHARMS USA
01 2INJECTABLE;INJECTION
02 1Injectable; Injection
03 18TABLET;ORAL
01 2DISCN
02 18RX
03 1Blank
01 4AZASAN
02 13AZATHIOPRINE
03 1AZATHIOPRINE SODIUM
04 3IMURAN
01 17No
02 3Yes
03 1Blank
RLD : No
TE Code : AB
Brand Name : AZASAN
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Approval Date : 1999-06-07
Application Number : 75252
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : AZASAN
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG
Approval Date : 2003-02-03
Application Number : 75252
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : AZATHIOPRINE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Approval Date : 1996-02-16
Application Number : 74069
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : AZATHIOPRINE
Dosage Form : TABLET;ORAL
Dosage Strength : 75MG
Approval Date : 2021-11-02
Application Number : 74069
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : No
TE Code : AB
Brand Name : AZATHIOPRINE
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Approval Date : 2021-11-02
Application Number : 74069
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
RLD : Yes
TE Code :
Brand Name : IMURAN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 17391
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : No
TE Code :
Brand Name : AZATHIOPRINE SODIUM
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/VIAL
Approval Date : 1995-03-31
Application Number : 74419
RX/OTC/DISCN : RX
RLD : No
TE Code :
RLD : Yes
TE Code : AB
Brand Name : IMURAN
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Approval Date : 1982-01-01
Application Number : 16324
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : IMURAN
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 16324
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD :
TE Code :
Brand Name : AZATHIOPRINE
Dosage Form : Injectable; Injection
Dosage Strength : EQ 100MG BASE/VIAL
Approval Date :
Application Number : 71056
RX/OTC/DISCN :
RLD :
TE Code :
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